Unbiased AI-powered news
Kalshi opened new markets on July 16 allowing bets on Phase 3 trial outcomes and full FDA drug approvals. The platform accepted more than $100,000 in wagers with trading volume at $128,401 by 3 p.m. EDT.
ForbesKalshi launched prediction markets on pharmaceutical clinical trial outcomes and FDA drug approvals on July 16 in partnership with AppliedXL. The markets permit bets on more than a dozen outcomes limited to Phase 3 trials by established biopharma companies and full FDA approval decisions. Trading volume in the medicine markets reached $128,401 by approximately 3 p.m.
EDT, and Kalshi accepted more than $100,000 in bets on the new markets by that date. Most available bets focus on late-stage trials by companies with market caps of at least $500 million. Specific markets include whether the FDA will approve Gilead Sciences' experimental cancer drug anito-cel by the end of 2026, whether AriBio's Alzheimer's drug will meet the goals of its late-stage clinical trial, and when Eli Lilly's weight-loss drug retatrutide will receive FDA approval.
One market asks whether the FDA will approve a cure for Type 1 diabetes before 2033, with 56 percent of bettors predicting no. Kalshi requires employment verification for traders and prohibits trading on material nonpublic information. Early-stage trials and conditional FDA approvals are excluded from the current markets.
These outlets didn't split into competing frames — coverage was uniform.
upi.comThe Food and Drug Administration approved enlicitide, sold as Lipfendra, on Thursday. Manufactured by Merck, the pill inhibits PCSK9 and cut LDL levels by up to 60 percent in a 24-week trial of 2,912 participants. It carries a list price of $315 for a 30-day supply and will reach…
washingtonpost.comFlooding along the Guadalupe River has killed at least one person in central Texas. The same area recorded more than 130 deaths in flash floods last summer. Governor Greg Abbott confirmed the fatality in a Thursday update.
dailywire.comKalshi will allow bets on selected clinical trial results and full FDA decisions, starting with Phase 3 studies from established companies. The FDA separately approved Merck's Lipfendra cholesterol pill based on studies showing up to 60% LDL reduction.